[S(R)]-N-[(1S)-1-[2-(Diadamantanphosphino)phenyl]ethyl]-2-methyl-2-propanesulfinamide

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Reagent Code: #68838
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CAS Number 1929530-56-2

science Other reagents with same CAS 1929530-56-2

blur_circular Chemical Specifications

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Weight 525.8 g/mol
Formula C₃₂H₄₈NOPS
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description Product Description

This chemical is primarily utilized in asymmetric synthesis, particularly as a chiral ligand or catalyst in transition metal-catalyzed reactions. Its unique structure, featuring diadamantylphosphine and sulfinamide groups, makes it highly effective in inducing enantioselectivity in various organic transformations. It is commonly employed in the synthesis of pharmaceutical intermediates, where precise control over stereochemistry is crucial. Additionally, it is used in the development of fine chemicals and specialty materials, enabling the production of compounds with high optical purity. Its robust and sterically demanding nature also makes it suitable for challenging catalytic processes, such as cross-coupling reactions and hydrogenations.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿6,201.00
inventory 100mg
10-20 days ฿11,781.00
inventory 500mg
10-20 days ฿43,200.00

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[S(R)]-N-[(1S)-1-[2-(Diadamantanphosphino)phenyl]ethyl]-2-methyl-2-propanesulfinamide
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This chemical is primarily utilized in asymmetric synthesis, particularly as a chiral ligand or catalyst in transition metal-catalyzed reactions. Its unique structure, featuring diadamantylphosphine and sulfinamide groups, makes it highly effective in inducing enantioselectivity in various organic transformations. It is commonly employed in the synthesis of pharmaceutical intermediates, where precise control over stereochemistry is crucial. Additionally, it is used in the development of fine chemicals an

This chemical is primarily utilized in asymmetric synthesis, particularly as a chiral ligand or catalyst in transition metal-catalyzed reactions. Its unique structure, featuring diadamantylphosphine and sulfinamide groups, makes it highly effective in inducing enantioselectivity in various organic transformations. It is commonly employed in the synthesis of pharmaceutical intermediates, where precise control over stereochemistry is crucial. Additionally, it is used in the development of fine chemicals and specialty materials, enabling the production of compounds with high optical purity. Its robust and sterically demanding nature also makes it suitable for challenging catalytic processes, such as cross-coupling reactions and hydrogenations.

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